A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985645



Internal ID57838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:77939972..77940023hg38UCSC Ensembl
chr6:78649689..78649740hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563219
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985645
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.183506


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